2009
DOI: 10.1248/bpb.32.2075
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Cytotoxic Constituents of Propolis from Myanmar and Their Structure-Activity Relationship

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Cited by 46 publications
(30 citation statements)
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“…Other studies showed that propolis ethanolic extract is cytotoxic on pulp fibroblasts [30] and cancer cells [31]. In the concentrations tested in this study, the cytotoxicity of the varnish containing propolis was considered low.…”
Section: Discussionmentioning
confidence: 89%
“…Other studies showed that propolis ethanolic extract is cytotoxic on pulp fibroblasts [30] and cancer cells [31]. In the concentrations tested in this study, the cytotoxicity of the varnish containing propolis was considered low.…”
Section: Discussionmentioning
confidence: 89%
“…Thirteen cycloartane-type triterpenes and four prenylated flavanones isolated from Myanmar propolis were evaluated. [60] A cycloartane-type triterpene, 3a,27-dihydroxycycloart-24E-en-26-oic acid, showed potent cytotoxicity against B16-BL6 murine melanoma cells, and (2S)-5,7-dihydroxy-4′-methoxy-8,3′-diprenylflavanone exhibited strong cytotoxic action against human cancer cell lines (lung A549 adenocarcinoma, cervix HeLa adenocarcinoma and HT-1080 fibrosarcoma). [60] A methanolic extract of propolis from Myanmar was found to inhibit PANC-1 human pancreatic cancer cells preferentially under nutrient-deprived conditions.…”
Section: Sh-sy5ymentioning
confidence: 99%
“…[60] A cycloartane-type triterpene, 3a,27-dihydroxycycloart-24E-en-26-oic acid, showed potent cytotoxicity against B16-BL6 murine melanoma cells, and (2S)-5,7-dihydroxy-4′-methoxy-8,3′-diprenylflavanone exhibited strong cytotoxic action against human cancer cell lines (lung A549 adenocarcinoma, cervix HeLa adenocarcinoma and HT-1080 fibrosarcoma). [60] A methanolic extract of propolis from Myanmar was found to inhibit PANC-1 human pancreatic cancer cells preferentially under nutrient-deprived conditions. Bioactivity-guided fractionation of the extract led to the isolation of cycloartanetype triterpenes (22Z,24E)-3-oxocycloart-22,24-dien-26-oic acid, which exhibited the most potent preferential cytotoxicity in a concentration-and time-dependent manner.…”
Section: Sh-sy5ymentioning
confidence: 99%
“…8-位具有 异戊烯基、法呢烯基、lavandylyl 的黄酮在多药耐药 [mutidrug resistance protein 1 (MRP1)/ATP-binding cassette C1(ABCC1) inhibitor]中更具有潜力 [57] . 增加异戊 烯基更是提高黄酮类化合物细胞毒活性的结构要求 [58] .…”
Section: 而黄酮醇的收率明显下降(Scheme 7)unclassified